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Entecavir Impurity 3

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For Research Use Only | Not For Clinical Use
CATAPB1391053943
CAS1391053-94-3
Molecular Weight293.28
Molecular FormulaC12H15N5O4

What is the name of the product associated with CAS 1391053-94-3?

The product name is Entecavir Impurity 3.

What is the molecular weight of Entecavir Impurity 3?

The molecular weight of Entecavir Impurity 3 is 293.28.

What is the molecular formula of Entecavir Impurity 3?

The molecular formula of Entecavir Impurity 3 is C12H15N5O4.

How is Entecavir Impurity 3 related to Entecavir?

Entecavir Impurity 3 is a chemical related to Entecavir, likely an impurity in the manufacturing process of Entecavir.

What is the significance of CAS number 1391053-94-3?

CAS number 1391053-94-3 is the unique identifier for Entecavir Impurity 3, allowing for easy reference and identification.

How is the purity of Entecavir Impurity 3 determined?

The purity of Entecavir Impurity 3 is likely determined through various analytical methods such as HPLC (High-Performance Liquid Chromatography).

Why is it important to identify and quantify impurities like Entecavir Impurity 3?

Identifying and quantifying impurities like Entecavir Impurity 3 is important for ensuring the quality, safety, and efficacy of the pharmaceutical product, in this case, Entecavir.

How are impurities like Entecavir Impurity 3 formed during the synthesis of pharmaceuticals?

Impurities like Entecavir Impurity 3 can be formed as byproducts of the chemical reactions involved in the synthesis of pharmaceuticals.

What are the potential risks associated with the presence of impurities like Entecavir Impurity 3 in pharmaceutical products?

Impurities like Entecavir Impurity 3 can potentially affect the stability, bioavailability, and overall safety of pharmaceutical products, leading to adverse effects in patients.

How can the presence of impurities like Entecavir Impurity 3 be minimized or eliminated in the production of pharmaceuticals?

To minimize or eliminate impurities like Entecavir Impurity 3, rigorous quality control measures, purification processes, and analytical testing can be implemented throughout the manufacturing process of pharmaceuticals.

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